Suppr超能文献

经导管主动脉瓣置换术:结果、适应症、并发症及创新

Transcatheter Aortic Valve Replacement: Outcomes, Indications, Complications, and Innovations.

作者信息

Young Michael N, Inglessis Ignacio

机构信息

Cardiology Division, Massachusetts General Hospital, Harvard Medical School, 55 Fruit Street, GRB8-852E, Boston, MA, 02114, USA.

出版信息

Curr Treat Options Cardiovasc Med. 2017 Sep 22;19(10):81. doi: 10.1007/s11936-017-0580-0.

Abstract

Transcatheter aortic valve replacement (TAVR) has become the standard of care for the treatment of severe aortic stenosis in individuals who are at prohibitive surgical risk and presents a viable alternative to surgery in selected patients who are at high operative risk. To date, outcomes from the PARTNER (Placement of AoRtic TraNscathetER Valve) and Medtronic CoreValve® US Pivotal trials continue to show the benefits of TAVR in these high-risk subgroups out to 5 and 3 years, respectively (as reported by Mack et al. Lancet. 85:2477-2484 2015; Kapadia et al. Lancet. 385:2485-2491 2015; Deeb et al. J Am Coll Cardiol. 67:2565-2574 2016). Furthermore, the recent release of the PARTNER-2 and SURTAVI trial results among other international data suggest that clinical outcomes for intermediate risk patients may be promising for TAVR compared to surgical aortic valve replacement (SAVR) (as reported by Leon et al. N Engl J Med. 374:1609-1620 2016; Reardon et al. N Engl J Med. 376:1321-1331 2017). However, several questions persist regarding TAVR-specific complications as well as long-term durability. Paravalvular regurgitation, permanent pacemaker implantation, stroke, vascular access injury, and renal failure in post-TAVR patients remain adversaries in the quest to perfect this groundbreaking, game-changing technology (as reported by Khatri et al. Ann Intern Med. 158:35-46 2013). In this review, we provide an up-to-date synopsis of results from landmark clinical trials that cumulatively attest to the comparability of TAVR to best medical therapy and SAVR in extreme-risk, high-risk, and intermediate-risk patient populations. We continue with a review of studies that seek to compare transcatheter vs. surgical valve implantation in lower-risk subgroups. We also introduce ongoing efforts to optimize the peri-procedural management of TAVR and conclude with a presentation of management strategies and new generation valve platforms that seek to address some of the current limitations of transcatheter valve implantation.

摘要

经导管主动脉瓣置换术(TAVR)已成为手术风险极高的严重主动脉瓣狭窄患者的标准治疗方法,并且为手术风险高的特定患者提供了一种可行的手术替代方案。迄今为止,来自PARTNER(主动脉经导管瓣膜植入)和美敦力CoreValve®美国关键试验的结果分别持续显示了TAVR在这些高危亚组中长达5年和3年的益处(如Mack等人在《柳叶刀》上发表的文章,2015年,第85卷,第2477 - 2484页;Kapadia等人在《柳叶刀》上发表的文章,2015年,第385卷,第2485 - 2491页;Deeb等人在《美国心脏病学会杂志》上发表的文章,2016年,第67卷,第2565 - 2574页)。此外,PARTNER - 2和SURTAVI试验结果以及其他国际数据的近期发布表明,与外科主动脉瓣置换术(SAVR)相比,TAVR在中度风险患者中的临床结局可能很有前景(如Leon等人在《新英格兰医学杂志》上发表的文章,2016年,第374卷,第1609 - 1620页;Reardon等人在《新英格兰医学杂志》上发表的文章,2017年,第376卷,第1321 - 1331页)。然而,关于TAVR特有的并发症以及长期耐用性仍存在一些问题。TAVR术后患者的瓣周反流、永久性起搏器植入、中风、血管通路损伤和肾衰竭仍然是完善这项开创性、改变游戏规则技术的挑战(如Khatri等人在《内科学年鉴》上发表的文章,2013年,第158卷,第35 - 46页)。在本综述中,我们提供了具有里程碑意义的临床试验结果的最新概要,这些结果累积证明了TAVR在极端风险、高风险和中度风险患者群体中与最佳药物治疗和SAVR的可比性。我们接着回顾了旨在比较低风险亚组中经导管瓣膜植入与外科瓣膜植入的研究。我们还介绍了正在进行的优化TAVR围手术期管理的努力,并以旨在解决经导管瓣膜植入当前一些局限性的管理策略和新一代瓣膜平台的介绍作为结尾。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验